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Protocol Active Surveillance Small Renal Masses (SRMs)

Primary Purpose

Kidney Cancer

Status
Recruiting
Phase
Not Applicable
Locations
Italy
Study Type
Interventional
Intervention
Active Surveillance
Sponsored by
IRCCS San Raffaele
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Kidney Cancer focused on measuring Kidney cancer, Active surveillance, Small renal masses, Partial nephrectomy

Eligibility Criteria

50 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. ability to read, understand and interpret an informed consent;
  2. voluntary subscription of the active surveillance protocol through written informed consent; 3) age over 50 years;

4) diagnosis of monolateral, monofocal, and first-rate solid renal mass less than 2 cm; 5) absence of symptoms due to renal tumor pathology.

Exclusion Criteria:

  1. patients with a history of previous renal neoplasia;
  2. monorenal patients;
  3. patients with hereditary renal tumors (such as tuberous sclerosis and Von Hippel Lindau syndrome, etc.);
  4. patients with metastasis;
  5. patients suffering from immunodepressive diseases;
  6. patients on concomitant therapy with chemotherapeutic agents or systemic immunosuppressants;
  7. patients with life expectancy of less than 1 year.

Sites / Locations

  • IRCCS San RaffaeleRecruiting

Arms of the Study

Arm 1

Arm Type

Other

Arm Label

Patients with small renal masses

Arm Description

Active surveillance

Outcomes

Primary Outcome Measures

Evaluate the therapeutic efficacy of active surveillance for small renal masses
Evaluate the therapeutic efficacy of active surveillance in patients with diagnosis of small renal tumor masses equal to or less than 2 cm in diameter.
Evaluate the proportion of patients who do not undergone active treatment
Proportion of patients who do not perform tumorectomy , tumor ablation or nephrectomy on the number of eligible patients that have been monitored for 12 months or more or have undergone surgery within 12 months

Secondary Outcome Measures

Incidence and nature of disease progression during the period active surveillance
Determine the incidence and nature of disease progression during the period of active surveillance; determine the annual growth rate of SRMs equal to or less than 2 cm of diameter; evaluate the appearance of symptoms associated with the disease (pain, haematuria) or syndrome paraneoplasty (fever, cachexia, hypercalcemia, polycythemia, granulocytosis); establish possible factors clinical, pathological and biological predictive of local or metastatic disease progression or that require surgery.
Evaluation of disease progression
The disease progression is defined as the growth of the maximum diameter of the renal mass equal to or more than 4 cm or doubling the tumor volume over a period of time ≤ 12 months. It is considered sign of progression also the vascular invasion, with the appearance of thrombosis of the renal vein or of the inferior vena cava;

Full Information

First Posted
January 11, 2019
Last Updated
February 10, 2020
Sponsor
IRCCS San Raffaele
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1. Study Identification

Unique Protocol Identification Number
NCT03804320
Brief Title
Protocol Active Surveillance Small Renal Masses (SRMs)
Official Title
Sorveglianza Attiva Dei Tumori Renali T1a Uguali o Inferiori a 2 cm
Study Type
Interventional

2. Study Status

Record Verification Date
February 2020
Overall Recruitment Status
Recruiting
Study Start Date
April 29, 2015 (Actual)
Primary Completion Date
December 11, 2023 (Anticipated)
Study Completion Date
December 11, 2028 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
IRCCS San Raffaele

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No

5. Study Description

Brief Summary
Prospective study of active surveillance, non-randomized, multicentric, in asymptomatic patients over the age of 50 years, not affected by other tumors, with occasional diagnosis of single monolateral solid renal mass equal to or less than 2 cm of diameter. Diagnosis will be performed with chest CT abdomen with contrast and / or MRI abdomen with Gadolinium (Gd); during the first year of active surveillance, the patient's status will be evaluated at 3, 6, 9 and 12 months from the diagnosis and, subsequently, according to the schedule of events shown in the table "Event Planning" At the end of the 5 years of follow up, the patient will be entrusted to his / her own treating physician, with indication to perform abdomen and chest x-ray echography every 6 months and thoracic abdomen TAC with contrast and / or MRI abdomen with (Gd) every 2 years up to 10 years from instrumental radiological diagnosis and registration and communication of the possible date of death and cause The primary caregivers and the patient will be contacted annually by the promoter center of the study at the end of the first 5 years of study follow up and the data will be entered in the database by the promoter center. The indication to surgical treatment or ablative treatment will be considered in the following cases: 1. appearance of metastasis 2. increase of the maximum diameter of the renal mass equal to or greater than 4 cm 3. time of doubling of the tumor mass size less than or equal to 12 months 4. appearance of symptoms associated with renal disease (pain, haematuria) 5. appearance of paraneoplastic syndrome (fever, cachexia, hypercalcemia, polycythemia, ranulocytosis) 6. willingness expressed by the patient to undergo surgery or ablative operation In the presence of at least one of the aforementioned criteria, the attending physician can evaluate the possible execution of renal biopsy. The finding of renal biopsy proved negative for neoplasia may allow the continuation of the active surveillance procedure undertaken, independently indi - ding from the presence of one of the above mentioned criteria. If the renal biopsy is negative, the therapeutic decision (continuation of the follow up within the protocol in question, surgery or exit from the protocol) will be agreed between the patient and the patient. In the case of a positive renal biopsy for renal neoplasia, the patient may be a candidate for renal tumorectomy / radical nephrectomy.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Kidney Cancer
Keywords
Kidney cancer, Active surveillance, Small renal masses, Partial nephrectomy

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
180 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Patients with small renal masses
Arm Type
Other
Arm Description
Active surveillance
Intervention Type
Other
Intervention Name(s)
Active Surveillance
Primary Outcome Measure Information:
Title
Evaluate the therapeutic efficacy of active surveillance for small renal masses
Description
Evaluate the therapeutic efficacy of active surveillance in patients with diagnosis of small renal tumor masses equal to or less than 2 cm in diameter.
Time Frame
10 years
Title
Evaluate the proportion of patients who do not undergone active treatment
Description
Proportion of patients who do not perform tumorectomy , tumor ablation or nephrectomy on the number of eligible patients that have been monitored for 12 months or more or have undergone surgery within 12 months
Time Frame
10 years
Secondary Outcome Measure Information:
Title
Incidence and nature of disease progression during the period active surveillance
Description
Determine the incidence and nature of disease progression during the period of active surveillance; determine the annual growth rate of SRMs equal to or less than 2 cm of diameter; evaluate the appearance of symptoms associated with the disease (pain, haematuria) or syndrome paraneoplasty (fever, cachexia, hypercalcemia, polycythemia, granulocytosis); establish possible factors clinical, pathological and biological predictive of local or metastatic disease progression or that require surgery.
Time Frame
10 years
Title
Evaluation of disease progression
Description
The disease progression is defined as the growth of the maximum diameter of the renal mass equal to or more than 4 cm or doubling the tumor volume over a period of time ≤ 12 months. It is considered sign of progression also the vascular invasion, with the appearance of thrombosis of the renal vein or of the inferior vena cava;
Time Frame
10 years

10. Eligibility

Sex
All
Minimum Age & Unit of Time
50 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: ability to read, understand and interpret an informed consent; voluntary subscription of the active surveillance protocol through written informed consent; 3) age over 50 years; 4) diagnosis of monolateral, monofocal, and first-rate solid renal mass less than 2 cm; 5) absence of symptoms due to renal tumor pathology. Exclusion Criteria: patients with a history of previous renal neoplasia; monorenal patients; patients with hereditary renal tumors (such as tuberous sclerosis and Von Hippel Lindau syndrome, etc.); patients with metastasis; patients suffering from immunodepressive diseases; patients on concomitant therapy with chemotherapeutic agents or systemic immunosuppressants; patients with life expectancy of less than 1 year.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Cristina Carenzi
Email
carenzi.cristina@hsr.it
First Name & Middle Initial & Last Name or Official Title & Degree
Roberto Bertini
Phone
+390226437267
Email
bertini.roberto@hsr.it
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Roberto Bertini
Organizational Affiliation
IRCCS San Raffaele
Official's Role
Principal Investigator
Facility Information:
Facility Name
IRCCS San Raffaele
City
Milan
ZIP/Postal Code
20132
Country
Italy
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Roberto Bertini
Phone
+390226437267
Email
bertini.roberto@hsr.it

12. IPD Sharing Statement

Plan to Share IPD
Undecided
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Protocol Active Surveillance Small Renal Masses (SRMs)

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